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Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy

Cancer immunotherapy is a novel therapeutic regimen because of the specificity and durability of immune modulations to treat cancers. Current cancer immunotherapy is limited by some barriers such as poor response rate, low tumor specificity and systemic toxicities. Porous nanomaterials (PNMs) posses...

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Autores principales: Li, Su-Ran, Huo, Fang-Yi, Wang, Han-Qi, Wang, Jing, Xu, Chun, Liu, Bing, Bu, Lin-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195345/
https://www.ncbi.nlm.nih.gov/pubmed/35701847
http://dx.doi.org/10.1186/s12951-022-01489-4
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author Li, Su-Ran
Huo, Fang-Yi
Wang, Han-Qi
Wang, Jing
Xu, Chun
Liu, Bing
Bu, Lin-Lin
author_facet Li, Su-Ran
Huo, Fang-Yi
Wang, Han-Qi
Wang, Jing
Xu, Chun
Liu, Bing
Bu, Lin-Lin
author_sort Li, Su-Ran
collection PubMed
description Cancer immunotherapy is a novel therapeutic regimen because of the specificity and durability of immune modulations to treat cancers. Current cancer immunotherapy is limited by some barriers such as poor response rate, low tumor specificity and systemic toxicities. Porous nanomaterials (PNMs) possess high loading capacity and tunable porosity, receiving intense attention in cancer immunotherapy. Recently, novel PNMs based drug delivery systems have been employed in antitumor immunotherapy to enhance tissue or organ targeting and reduce immune-related adverse events. Herein, we summarize the recent progress of PNMs including inorganic, organic, and organic–inorganic hybrid ones for cancer immunotherapy. The design of PNMs and their performance in cancer immunotherapy are discussed in detail, with a focus on how those designs can address the challenges in current conventional immunotherapy. Lastly, we present future directions of PNMs for cancer immunotherapy including the challenges and research gaps, providing new insights about the design of PNMs for efficient cancer immunotherapy with better performance as powerful weapons against tumors. Finally, we discussed the relevant challenges that urgently need to be addressed in clinical practice, coupled with corresponding solutions to these problems.
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spelling pubmed-91953452022-06-15 Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy Li, Su-Ran Huo, Fang-Yi Wang, Han-Qi Wang, Jing Xu, Chun Liu, Bing Bu, Lin-Lin J Nanobiotechnology Review Cancer immunotherapy is a novel therapeutic regimen because of the specificity and durability of immune modulations to treat cancers. Current cancer immunotherapy is limited by some barriers such as poor response rate, low tumor specificity and systemic toxicities. Porous nanomaterials (PNMs) possess high loading capacity and tunable porosity, receiving intense attention in cancer immunotherapy. Recently, novel PNMs based drug delivery systems have been employed in antitumor immunotherapy to enhance tissue or organ targeting and reduce immune-related adverse events. Herein, we summarize the recent progress of PNMs including inorganic, organic, and organic–inorganic hybrid ones for cancer immunotherapy. The design of PNMs and their performance in cancer immunotherapy are discussed in detail, with a focus on how those designs can address the challenges in current conventional immunotherapy. Lastly, we present future directions of PNMs for cancer immunotherapy including the challenges and research gaps, providing new insights about the design of PNMs for efficient cancer immunotherapy with better performance as powerful weapons against tumors. Finally, we discussed the relevant challenges that urgently need to be addressed in clinical practice, coupled with corresponding solutions to these problems. BioMed Central 2022-06-14 /pmc/articles/PMC9195345/ /pubmed/35701847 http://dx.doi.org/10.1186/s12951-022-01489-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Li, Su-Ran
Huo, Fang-Yi
Wang, Han-Qi
Wang, Jing
Xu, Chun
Liu, Bing
Bu, Lin-Lin
Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
title Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
title_full Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
title_fullStr Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
title_full_unstemmed Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
title_short Recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
title_sort recent advances in porous nanomaterials-based drug delivery systems for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195345/
https://www.ncbi.nlm.nih.gov/pubmed/35701847
http://dx.doi.org/10.1186/s12951-022-01489-4
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